2015
DOI: 10.1186/1471-2164-16-s3-s1
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Identifying essential proteins from active PPI networks constructed with dynamic gene expression

Abstract: Essential proteins are vitally important for cellular survival and development, and identifying essential proteins is very meaningful research work in the post-genome era. Rapid increase of available protein-protein interaction (PPI) data has made it possible to detect protein essentiality at the network level. A series of centrality measures have been proposed to discover essential proteins based on the PPI networks. However, the PPI data obtained from large scale, high-throughput experiments generally contai… Show more

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Cited by 71 publications
(41 citation statements)
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“…The raw reads were evaluated by FastQc (Nanjing Agricultural University, Nanjing, China) to ensure that high-quality data could be obtained [54], and the raw reads were cleaned by filtering the adapter and low-quality reads using Trimmomatic (version 0.36, Nanjing Agricultural University, Nanjing, China) [54]. Then, the high-quality clean reads were mapped to the pig reference genome (Sus scrofa 11.1, http://ftp.ensemblorg.ebi.ac.uk/pub/release-93/fasta/sus_scrofa/dna/) using the HISAT2 version 2.0.1 (Iowa State University, Ames, IA, USA) with the default parameters [16,55,56], and using SAMtools (version 0.1.19,Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK) to sort and convert the SAM files to BAM [16].…”
Section: Rna-seq Reads Mapping and Transcriptome Assemblymentioning
confidence: 99%
“…The raw reads were evaluated by FastQc (Nanjing Agricultural University, Nanjing, China) to ensure that high-quality data could be obtained [54], and the raw reads were cleaned by filtering the adapter and low-quality reads using Trimmomatic (version 0.36, Nanjing Agricultural University, Nanjing, China) [54]. Then, the high-quality clean reads were mapped to the pig reference genome (Sus scrofa 11.1, http://ftp.ensemblorg.ebi.ac.uk/pub/release-93/fasta/sus_scrofa/dna/) using the HISAT2 version 2.0.1 (Iowa State University, Ames, IA, USA) with the default parameters [16,55,56], and using SAMtools (version 0.1.19,Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK) to sort and convert the SAM files to BAM [16].…”
Section: Rna-seq Reads Mapping and Transcriptome Assemblymentioning
confidence: 99%
“…A limitation of our analysis is that we did not make any adjustment for ancestry admixture/population structure. In genetic association studies of admixed populations such as Mexican Americans, addressing differential ancestral backgrounds is important to avoid false positive or negative association signals [14, 15]. …”
Section: Discussionmentioning
confidence: 99%
“…org/) [33], iRefIndex (http://irefindex.org/wiki/index.php?title=iRefIndex) [34], STRING (https://stringdb.org/) [35], MatrixDB (http://matrixdb.univ-lyon1.fr/) [36], MPIDB (https://www.jcvi.org/mpidb/ about.php) [37], InnateDB (https://www.innatedb.com/) [38], iRefWeb (http://wodaklab.org/iRefWeb/ search/index) [39], I2D (http://ophid.utoronto.ca/ophidv2.204/) [40] and converted the results visually by using Cytoscape software (http://www.cytoscape.org/) [41]. Topological properties of PPI network such as node degree [42], betweenness [43], stress [44], closeness [45] and clustering coefficient [46] were calculated. Furthermore, module analysis was performed by using the PEWCC1 [47] plugin (version 1.3) to explore the most important clustering modules in the huge PPI network (degree cutoff = 5, k-core = 2, node score cutoff = 0.2, and max.…”
Section: Comprehensive Analysis Of Ppi Network and Modulesmentioning
confidence: 99%